A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv893610



Internal ID6300621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100327598..100482976hg19UCSC Ensembl
Outerchr9:100324086..100496160hg19UCSC Ensembl
Innerchr9:99367419..99522797hg18UCSC Ensembl
Outerchr9:99363907..99535981hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1587045
SamplesIS37986
Known GenesNCBP1, TMOD1, TSTD2, XPA
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv893610
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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